WO2011153460A2 - Amibes thérapeutiques et leurs utilisations - Google Patents

Amibes thérapeutiques et leurs utilisations Download PDF

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Publication number
WO2011153460A2
WO2011153460A2 PCT/US2011/039110 US2011039110W WO2011153460A2 WO 2011153460 A2 WO2011153460 A2 WO 2011153460A2 US 2011039110 W US2011039110 W US 2011039110W WO 2011153460 A2 WO2011153460 A2 WO 2011153460A2
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Prior art keywords
amoebae
bacteria
microorganism
species
subject
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PCT/US2011/039110
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English (en)
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WO2011153460A3 (fr
Inventor
Marcin Filutowicz
Katarzyna Dorota Borys
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Amebagone, Llc
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Priority to EP11790485.4A priority Critical patent/EP2575833B1/fr
Publication of WO2011153460A2 publication Critical patent/WO2011153460A2/fr
Publication of WO2011153460A3 publication Critical patent/WO2011153460A3/fr

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    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N63/00—Biocides, pest repellants or attractants, or plant growth regulators containing microorganisms, viruses, microbial fungi, animals or substances produced by, or obtained from, microorganisms, viruses, microbial fungi or animals, e.g. enzymes or fermentates
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
    • A61K35/66—Microorganisms or materials therefrom
    • A61K35/68—Protozoa, e.g. flagella, amoebas, sporozoans, plasmodium or toxoplasma
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/10—Antimycotics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Definitions

  • the present invention relates to amoebae (slime molds) and uses thereof.
  • the present invention relates to the use of amoebae or their environmentally stable spores to treat microbial infections and other uses.
  • MRSA methicillin resistant Staphylococcus aureus
  • MDR multi-drug resistant Acinetobacter baumannii
  • MRSA are becoming increasingly resistant to tetracyclines, fluoroquinolones, clindamycin, and vancomycin, and these antibiotics are rapidly becoming non-effective treatments (Kaka AS, et al. 2006. J Antimicrob Chemother. 58:680-683). Furthermore, sulfamethoxazole-trimethoprim has recently been shown to have a treatment failure rate of fifty-percent (Proctor RA. 2008. Clin Infect Dis. 46:584-593).
  • MDR baumannii The situation for MDR baumannii is also troubling. MDR strains of this organism have been isolated that are resistant to all approved frontline and secondary antibiotics (Maragakis LL & Perl TM. 2008. Clin Infect Dis. 46: 1254-1263). Without effective treatments, patients with MRSA or MDR A. baumannii infections have longer periods of hospitalization, increased morbidity, and a greater likelihood of in-hospital death (Bassetti M, et al. 2009. Fut Microbiol. 3:649-660; Frazee BW, et al. 2005. Ann Emerg Med. 45:311-320).
  • Antibiotic resistance problem is not limited in its scope to medical settings. Antibiotic uses and misuses in veterinary science and in agriculture are a global and rapidly growing issue. For example, "fire blight, caused by Erwinia amylovora, is a major threat to apple and pear production worldwide. Nearly all pear varieties and many of the most profitable apple varieties and horticulturally-desirable rootstocks planted throughout the U.S. are highly susceptible to fire blight. Therefore, most growers apply the antibiotics streptomycin or oxytetracycline one to three times during bloom to prevent growth of E. amylovora.
  • the present invention relates to amoebae (slime molds) and uses thereof.
  • the present invention relates to the use of amoebae or their environmentally stable spores to treat microbial infections and other uses.
  • the present invention provides a method of killing or slowing the rate of growth of a microorganism (e.g., treating a microbial infection), comprising: contacting a microoroganism with a composition (e.g., a pharmaceutical composition) comprising one or more species of amoebae, wherein the contacting kills or slows the growth of the microorganism.
  • a microoroganism e.g., a pharmaceutical composition
  • the microorganism is a bacteria (e.g., a pathogenic bacteria such as MRS A, multi-drug resistant bacteria or persister cells of a bacteria) or a fungus.
  • the microorganisms are present in planctonic or bio film forms.
  • the microorganism is in or on a subject.
  • the microorganism is present in a wound, a mucus membrane (e.g., nostril, throat, rectum, vagina, etc.), a tissue or an organ of the subject.
  • the wound is at a temperature above the normal body temperature of the subject or is hypoxic.
  • the microorganism is in or on a plant (e.g., an agricultural or industrial plant).
  • the composition comprises two or more species of amoebae.
  • the present invention is not limited to a particular strain or species of amoebae. Examples include, but are not limited to, Polyspondillum palidum Salvador, ibid WS 371A, D. discoideum WS 647, Dictyostelium giganteum WS 142, Turkey 27,
  • composition further comprises a non-amoebae anti-microbial agent, along with one or more carriers or other components.
  • Certain embodiments of the invention provide a method of treating a subject (e.g., a human) infected with a microorganism, comprising: contacting a subject infected with a microoroganism with a pharmaceutical composition comprising one or more species of amoebae, wherein the contacting kill the microorganism.
  • a subject e.g., a human
  • a pharmaceutical composition comprising one or more species of amoebae
  • compositions comprising: one or more species of amoebae; and a carrier (e.g., a
  • the present invention provides for the use of a pharmaceutical composition comprising a) one or more species of amoebae; and b) a pharmaceutically acceptable carrier in the treatment of a subject infected with a microorganism.
  • Figure 1 shows a photograph of feeding amoebae.
  • Figure 2 shows an electron micrograph showing several stages of amoebic phagocytosis. (Clockwise from the top): Free Klebsiella aerogenes; D. discoideum forms a cup structure and begins to engulf the bacteria. The bacteria, sequestered within a phagosome are digested (image reproduce from Cohen ML. 2000. Nature. 406: 762-767).
  • Figure 3 shows a) development stages of soil-borne amoeba and b) lifecycle of D. discoideum (Modified from Science 325: 1199).
  • the social amoebae belonging to the phylum Mycetozoa have been described as primitive eukaryotes that exhibit characteristics found among both protozoans and fungi (Bonner JT. (2009) The social amoebae: the biology of cellular slime molds; Raper et al, (1984) The Dictyostelids). This description can be summarized in an illustration of their asexual life cycle.
  • amoeba has a vegetative phase where, as microscopic unicellular protists, independent amoeboid cells feed upon bacteria, grow, and multiply.
  • the amoebae exhaust their bacterial food source, they enter a social phase in which individual cells stream together to form a multicellular, differentiated, mobile slug. Since growth occurred at the single-cell stage, its size depends on how many amoebae have entered the aggregate, and slugs will vary in length from about 0.2 to 2 millimeters, a ten fold range, and by the latest estimates the number of amoebae they contain ranges from about 10,000 to 2 million .
  • the slug eventually comes to rest and develops into a macroscopic fruiting body consisting of a stalk with sorocarp.
  • sorocarp Within the sorocarp are environmentally and temporally stable spores, which are disseminated by the wind, animals, or the forces generated by the sorocarp falling. From each viable spore a single amoeba arises.
  • Figure 4 shows a photograph of killing of bacteria by amoebae; formation of clearing zones also known as "plaques.”
  • Figure 5 shows synergism versus antagonism between various kinds of amoebae feeding on K. pneumonia.
  • Figure 6 shows intraspecies variation in amoebic tolerance of hypoxia. Pictured are three tubes containing semi-solid media inoculated with Klebsiella pneumoniae.. Tube (A) was an amoebae-free control. Tube (B) was co-inoculated with D. discoideum WI647. The arrow points to a clear band created as the burrowing amoebae consumed bacteria. Oxygen tension is lower within the medium than at the surface. Tube (C) was co-inoculated with D. discoideum X3. This isolate formed plaques on plates seeded with K. pneumonia, indicating that the amoebae can feed and are motile, but no band of bacterial clearing was observed in the tube.
  • A was an amoebae-free control.
  • Tube (B) was co-inoculated with D. discoideum WI647
  • Figure 7 shows Growth/sporulation of various amoebae on wild-type (top) and menD mutant (bottom) of S. aureus. Some amoebae not only feed on bacteria on the plate surface but undergo a full development (middle horizontal panel).
  • Figure 8 shows feeding of amoebae on Erwinia amylovora grown in SM2 medium "impregnated" with a slice of a pear. As indicated the plate surface was inoculated either with spores or with amoebae. Two amoebae isolates were tested, X3 and WS 321.7
  • Figure 9 shows growth of amoebae at temperatures encountered in skin wounds.
  • Figure 10 shows feeding of amoebae on MRS A on non-nutrient agar in the presence of serum.
  • Figure 11 shows a comparison of the feeding of amoebae on Klebsiella pneumoniae with and without serum.
  • Figure 12 shows feeding of amoebae on a menD mutant of S. aureus in presence and absence of serum.
  • Figure 13 shows feeding of amoebae on Wide Type Staphylococcus in presence or absence of serum.
  • Figure 14 shows feeding of amoebae on natural isolates of virulent strains of Erwinia amylovora (88, 85.1 and A97.1) a causative agent of Fire blight in fruit crops.
  • Figure 15 shows feeding of amoebae on natural isolate virulent agent of bean disease Pseudomonas syringe 207.2.
  • Medical devices includes any material or device that is used on, in, or through a subject's or patient's body, for example, in the course of medical treatment (e.g., for a disease or injury).
  • Medical devices include, but are not limited to, such items as medical implants, wound care devices, drug delivery devices, birth control and body cavity and personal protection devices.
  • medical implants include, but are not limited to, urinary catheters, intravascular catheters, dialysis shunts, wound drain tubes, skin sutures, vascular grafts, implantable meshes, intraocular devices, heart valves, and the like.
  • Wound care devices include, but are not limited to, general wound dressings, biologic graft materials, tape closures and dressings, and surgical incision drapes.
  • Drug delivery devices include, but are not limited to, needles, drug delivery skin patches, drug delivery mucosal patches and medical sponges.
  • Body cavity and personal protection devices include, but are not limited to, tampons, sponges, surgical and examination gloves, and toothbrushes.
  • birth control devices include, but are not limited to, intrauterine devices (IUDs), diaphragms, and condoms.
  • therapeutic agent refers to compositions (e.g., comprising amoebae) that decrease the infectivity, morbidity, or onset of mortality in a subject contacted by a pathogenic microorganism or that prevent infectivity, morbidity, or onset of mortality in a host contacted by a pathogenic microorganism.
  • therapeutic agents encompass agents used prophylactically, e.g., in the absence of a pathogen, in view of possible future exposure to a pathogen.
  • agents may additionally comprise
  • the therapeutic agents of the present invention are administered in the form of topical compositions, injectable compositions, ingestible compositions, and the like.
  • the form may be, for example, a solution, cream, ointment, salve or spray.
  • pathogen refers to a biological agent that causes a disease state (e.g., infection, cancer, etc.) in a host.
  • pathogens include, but are not limited to, bacteria, fungi, archaea, protozoans, mycoplasma, and other parasitic organisms.
  • microorganism refers to any species or type of
  • microorganism including but not limited to, bacteria, archea, fungi, protozoans, mycoplasma, and parasitic organisms.
  • the present invention contemplates that a number of
  • microorganisms encompassed therein will also be pathogenic to a subject.
  • bacteria and "bacterium” refer to all prokaryotic organisms, including those within all of the phyla in the Kingdom Procaryotae. It is intended that the term encompass all microorganisms considered to be bacteria including Mycoplasma, Chlamydia, Actinomyces, Streptomyces, and Rickettsia. All forms of bacteria are included within this definition including cocci, bacilli, spirochetes, spheroplasts, protoplasts, etc. Also included within this term are prokaryotic organisms that are gram negative or gram positive. "Gram negative” and “gram positive” refer to staining patterns with the Gram-staining process that is well known in the art.
  • Gram positive bacteria are bacteria that retain the primary dye used in the Gram stain, causing the stained cells to appear dark blue to purple under the microscope.
  • Gram negative bacteria do not retain the primary dye used in the Gram stain, but are stained by the counterstain. Thus, gram negative bacteria appear red.
  • the bacteria are those capable of causing disease (pathogens) and those that cause production of a toxic product, tissue degradation or spoilage.
  • fungi is used in reference to eukaryotic organisms such as the molds and yeasts, including dimorphic fungi.
  • non-human animals refers to all non-human animals including, but are not limited to, vertebrates such as rodents, non-human primates, ovines, bovines, lagomorphs, porcines, caprines, equines, canines, felines, aves, etc.
  • biofilm refers to an aggregation of microorganisms (e.g., bacteria) surrounded by an extracellular matrix or slime adherent on a surface in vivo or ex vivo, wherein the microorganisms adopt altered metabolic states.
  • microorganisms e.g., bacteria
  • the term "subject” refers to organisms to be treated by the methods of embodiments of the present invention. Such organisms preferably include, but are not limited to, mammals ⁇ e.g., murines, simians, equines, bovines, porcines, canines, felines, and the like), and most preferably includes humans.
  • the term “subject” generally refers to an individual who will receive or who has received treatment ⁇ e.g. , administration of a amoebae of the present invention and optionally one or more other agents) for a condition characterized by infection by a microorganism or risk of infection by a microorganism.
  • diagnosis refers to the recognition of a disease by its signs and symptoms ⁇ e.g., resistance to conventional therapies), or genetic analysis, pathological analysis, histological analysis, diagnostic assay (e.g., for microorganism infection) and the like.
  • in vitro refers to an artificial environment and to processes or reactions that occur within an artificial environment. In vitro environments include, but are not limited to, test tubes and cell cultures.
  • in vivo refers to the natural environment ⁇ e.g., an animal or a cell) and to processes or reaction that occur within a natural environment.
  • host cell refers to any eukaryotic or prokaryotic cell (e.g., mammalian cells, avian cells, amphibian cells, plant cells, fish cells, and insect cells), whether located in vitro or in vivo.
  • cell culture refers to any in vitro culture of cells. Included within this term are continuous cell lines (e.g., with an immortal phenotype), primary cell cultures, finite cell lines (e.g., non-transformed cells), and any other cell population maintained in vitro, including oocytes and embryos.
  • the term “genome” refers to the genetic material (e.g., chromosomes) of an organism or a host cell.
  • an effective amount refers to the amount of a therapeutic agent (e.g., an amoebae) sufficient to effect beneficial or desired results.
  • An effective amount can be administered in one or more administrations, applications or dosages and is not intended to be limited to a particular formulation or administration route.
  • co-administration refers to the administration of at least two agent(s) (e.g., an amoeba) or therapies to a subject. In some embodiments, the coadministration of two or more agents/therapies is concurrent. In some embodiments, a first agent/therapy is administered prior to a second agent/therapy.
  • agents/therapies used may vary.
  • the appropriate dosage for co-administration can be readily determined by one skilled in the art.
  • the respective agents/therapies are administered at lower dosages than appropriate for their administration alone.
  • co-administration is especially desirable in embodiments where the co-administration of the agents/therapies lowers the requisite dosage of a known potentially harmful (e.g., toxic) agent(s).
  • the term "toxic” refers to any detrimental or harmful effects on a cell or tissue as compared to the same cell or tissue prior to the administration of the toxicant.
  • composition refers to the combination of an active agent with a carrier, inert or active, making the composition especially suitable for diagnostic or therapeutic use in vivo, in vivo or ex vivo.
  • the term "pharmaceutically acceptable carrier” refers to any of the standard pharmaceutical carriers, such as a phosphate buffered saline solution, water, emulsions (e.g., such as an oil/water or water/oil emulsions), and various types of wetting agents.
  • the compositions also can include stabilizers and preservatives.
  • stabilizers and adjuvants See e.g., Martin, Remington's Pharmaceutical Sciences, 15th Ed., Mack Publ. Co., Easton, PA [1975]).
  • sample as used herein is used in its broadest sense.
  • a sample may comprise a cell, tissue, or fluids, nucleic acids or polypeptides isolated from a cell (e.g., a microorganism), and the like.
  • the terms “purified” or “to purify” refer, to the removal of undesired components from a sample.
  • substantially purified refers to molecules that are at least 60% free, preferably 75% free, and most preferably 90%, or more, free from other components with which they usually associated.
  • module refers to the activity of a compound (e.g., an amoebae) to affect (e.g., to kill or prevent the growth of) a microorganism.
  • a compound e.g., an amoebae
  • test compound refers to any chemical entity, pharmaceutical, drug, and the like, that can be used to treat or prevent a disease, illness, sickness, or disorder of bodily function, or otherwise alter the physiological or cellular status of a sample (e.g., infection by a microorganism).
  • Test compounds comprise both known and potential therapeutic compounds.
  • a test compound can be determined to be therapeutic by using the screening methods of the present invention.
  • a "known therapeutic compound” refers to a therapeutic compound that has been shown (e.g. , through animal trials or prior experience with administration to humans) to be effective in such treatment or prevention.
  • test compounds are agents that treat or prevent infection by a
  • the present invention relates to amoebae (slime molds) and uses thereof.
  • the present invention relates to the use of amoebae or their environmentally stable spores to treat microbial infections and other uses.
  • Embodiments of the present invention provide for the use of amoebae (slime molds) in treatment and prevention of microbial infection, in particular, against some of the most tenacious pathogens.
  • amoebae slime molds
  • amoebae slime molds
  • amoebae offer many of the same advantages as maggots, while their microscopic, spore-forming lifestyle and the parallels to be drawn with phagocytic immune cells make them more appealing, less expensive to make, and more convenient to use.
  • amoebic therapy derives from amoebae (or their spores) being an easily transported and applied antibacterial agent, effective against a broad range of pathogens including drug resistant bacteria.
  • amoebae feeding on bacteria finds use for application at non-sterile sites (e.g. the skin or mucosal surfaces). At these sites, overwhelming numbers of amoebae are used to quickly consume pathogenic bacteria. Since amoebae possess the ability to consume wound bacteria, especially pathogens that are impervious to chemical antibiotics, they further find use as an effective prophylactic, an adjunct to current therapies, or an independent remedy. In some embodiments, amoebae (or their germinating spores) are applied to infected tissue where they quickly reduce the microbial load and, in doing so, promote healing.
  • the patient populations that benefit from this form of therapy are those with, for example, diabetic skin lesions, burns, and surgical or chance wounds.
  • Amoebae further find use in a variety of additional applications. Examples include, but are not limited to, veterinary science, agriculture, food industry and industrial settings (e.g., prevention or remediation of fouling of machine parts, water lines, medical devices, etc.).
  • amoeba When a few spores are added, in a matter of hours they split open and from each spore emerges a single amoeba that immediately begins to feed on the surrounding bacteria. As they grow they divide in two (e.g., approximately every three hours) so vast numbers of amoebae are soon present.
  • Each individual amoeba surrounds a bacterium (or other microorganism) with its pesudopods, encases it in a food vacuole, and extracts the needed nutrients.
  • amoebae can be viewed as professional phagocytes that are similar to macrophages and neutrophils (Chen G, et al. 2007. Science. 317:678-68).
  • both amoebae and the immune cells capture bacteria by phagocytosis within cytoplasmic vesicles ( Figure 2). These vesicles fuse with lysosomes as a step in the killing of entrapped bacteria.
  • amoebae clean an area of bacteria, they then come together and aggregate to form a unit similar to a multi-cellular organism.
  • thousands of amoebae aggregate in tune to a camp signal and the single cells form a slug.
  • amoebae When the amoebae exhaust their bacterial food source, they enter a social phase in which individual cells stream together to form a multicellular, differentiated, mobile slug. Since growth occurs at the single-cell stage, its size depends on how many amoebae have entered the aggregate, and slugs will vary in length from about 0.2 to 2 millimeters, a ten fold range, and by the latest estimates the number of amoebae they contain ranges from about 10,000 to 2 million. The slug eventually comes to rest and develops into a macroscopic fruiting body consisting of a stalk with sorocarp. Within the sorocarp are environmentally and temporally stable spores, which are disseminated by the wind, animals, or the forces generated by the sorocarp falling. From each viable spore a single amoeba arises
  • amoebae Unlike animals or plants, amoebae eat first; then grow by simply producing an increasing number of separate amoebae, and when food (bacteria/fungi) is gone they stream together to become multi-cellular. Once amoebae form their fruiting bodies they can no longer do anything that requires an intake of energy: they are static. The only part of them that is alive is the dormant spores.
  • amoebae possess many other virtues that are conducive to an amoebic antimicrobial therapy: Most prominent virtues of this group of organisms have been studied and extensively described for Dictyostelium discoideum.
  • D. discoideum amoebae and spores themselves are not known to be pathogenic to animals and plants. D. discoideum consumes and digests a variety of pathogenic and nonpathogenic bacteria, whether live or dead. Moreover, bacteria that are resistant to
  • amoeba are prophylactically administered to patients who are at a high risk of infection (e.g. hospitalized burn patients), that risk unacceptable consequences of infections (e.g. after cosmetic surgery), or who are injured in high risk environments like battlefields.
  • D. discoideum amoeba is not susceptible to anti-prokaryotic antibiotics. Therefore, amoebae can be used in conjunction with most of the antibiotics used to treat bacterial infections.
  • amoebae As a phagocytic agent, amoebae internally digest bacteria. Unlike conventional antibiotics, toxic bacterial products are contained and digested within cytoplasmic vesicles. Thus, endotoxic shock reactions seen in patients treated with conventional antibiotics are unlikely following amoebic therapy (Prins JM, et al. 1994. Antimicrob Agent Chemother. 38(6): 1211-1218).
  • amoebic therapy utilizes overwhelming numbers of amoebae. Locally, these amoebae quickly contain and consume their bacterial prey.
  • the present invention is not limited to a particular mechanism. Indeed, an understanding of the mechanism is not necessary to practice the present invention. Nonetheless, it is contemplated that in the time frame of therapy, resistance to amoebae will be difficult for pathogens to acquire, and spread of resistance will be minimized.
  • Certain bacteria are facultative intracellular pathogens and there are known strain of genetically engineered bacteria, like the benign soil bacterium Bacillus subtilis harboring the gene for lysteriolysin O, can survive within macrophage-like cell line (Bielecki J, et al. 1990. Nature, 345: 175-176).
  • resistance to amoebic therapy can be minimized or eliminated.
  • embodiments of the present invention provide compositions and methods for treating infection by microorganisms with amoebae.
  • amoebae suitable for use in embodiments of the present invention include, but are not limited to, amoebae of the phylum Mycetozoa, which include but are not limited to:
  • DICTYOSTELIUM D. laterosorum, D. rion, D. potamoides, D.minutum, D.gracile, D. lavandulum, D. vinaceo-fuscum, D. rhizopodium, D. coeruleo-stipes, D.lacteum, D.
  • polycephalum D. polycarpum, D. polycarpum, D. menorah, D. caveatum, D. gloeosporum, D. oculare, D. antarcticum, D. fasciculatum, D. americanum, D. fasciculatum, D.aureo-stipes var. helveticum, D. granulophorum, D. medusoides, D. mexicanum, D. bifurcatum, D.
  • D.discoideum D. discoideum AX4, D. intermedium, D. firmibasis, D. brunneum,
  • pseudocandidum P. tenuissimum, P. pallidum, P. asymmetricum, P. filamentosum, P.
  • longisorophorum A. leptosomum, A. digitatum, A. serpentarium, A. subglobosum, A.
  • ACRASIDE A. granulate, A. rosea
  • COPROMYXA C. protea, C.
  • GUTTULINOPSIS G. vulgaris, G. clavata, G. stipitata, G. nivea See e.g., Schaap, et al. 2006 Molecular Phylogeny and Evolution of Morphology in the Social Amoebas, Science 27 October 2006: 661-663; Raper KB. 1984. The Dictyostelids. Princeton University Press. Princeton NJ; each of which is herein incorporated by reference in its entirety).
  • Polispondillum candidum Frl4 all names, except D. discoideum X3, given by K. Raper in his collection of slime molds maintained by and available at the Department of Bacteriology at University of Wisconsin-Madison, USA).
  • a dichotomous key based on cellular morphology and behavior plus the shape and color of spores, sori, or sorocarp has been used to determine the genus and species of the Mycetozoa (Raper KB, Rahn AW.
  • amoebae described herein have evolved to consume a myriad of species of bacteria that live in soil communities. Like macrophages and neutrophils, single celled amoebae chase, engulf and digest their microbial prey (Chen G, Zhuchenko O, Kuspa A. (2007) Science 317(5838): 678-81). Amoebae readily consume planktonic bacteria. In addition, they likely have acquired the ability to eat bacteria within biofilms because amoebae thrive within biologically complex and environmentally harsh soil bio-webs (Rodriguez S, Bishop P. (2007) Three-dimensional quantification of soil biofilms using image analysis. Environ Eng Sci 24(2): 96-103).
  • D. discoideum isolates are utilized. Strains of amoebae have been isolated that grow on bacteria and on synthetic media (Sussman M, 1966. Biochemical and genetic methods in the study of cellular slime mold development, pp. 397-410. In:
  • D. discoideum is a haploid easing the genetic characterization of mutant organisms; the genome sequence of D. discoideum has been determined and published (Eichinger L, et al. 2005. Nature. 435:43-57). Also, that genome was recently compared to the genome of the genomes sequence of D. purpureum (R. Sucgang et al, 2011, Genome Biology 2011, 12).
  • amoeba therapy utilizes D. discoideum isolate AX-3, but is not limited to this axenic strain.
  • AX-3 isolate has the novel, and useful, property of axenic growth; that is, growth on media without a bacterial food supply.
  • AX-3 is predated by other axenic mutants. Repeated sub-culturing of wild type D. discoideum in a liquid medium containing salts, liver extract, and fetal calf serum was used to obtain archetype axenic strains. Using this technique, Sussman and Sussman isolated AX-1, the first reported axenic mutant (Sussman R & Sussman M. 1967. Biochem. Biophys. Res. Commun.
  • Advantageous phenotypes can be linked to multiple genetic mutations, and these mutations can be serially selected using multiple rounds of MNNG mutagenesis.
  • Most questions concerning amoebic therapy can be addressed by manipulating of the amoeba's genome.
  • Amoeba can be genetically altered by chemical mutagenesis or with molecular techniques.
  • D. discoideum is a haploid organism. Its genome sequence is published and mutants are easily generated by chemical mutagenesis, gene replacement technologies, and by RNA interference (Barclay SL & Meller E. 1983. Mol Cell Biol.
  • amoebae are stored and/or transported in the spore stage of the life cycle.
  • D. discoideum forms easily germinated temperature-, environment-, and temporally-stable spores. In the absence of a bacterial food supply, essential amino acids become limiting, and D. discoideum sporulates. Spores have been shown to remain viable, without refrigeration, for over 50 years when lyophilized or stored in silica gel. When nutrients are available, spores germinate in 6 - 10 hours to produce amoebae. Spores can be exploited as a means of transport and storage of medicinal amoebae. For convenience, spores can be administered embedded in bandages or dressings, gels, etc.
  • kits and/or compositions comprising amoebae.
  • amoebae are in a form (e.g., spores) that is stable for long term storage.
  • amoebae are stored and transported in different stages.
  • compositions comprise additional components (e.g., storage reagents, buffers, preservatives, stabilizers, etc.).
  • amoeba or spores are stored or transported at 80°C in 10% Dimethyl sulfoxide (DMSO) or 10% glycerol, in the MS2 medium comprising the following: peptone 10 g, dextrose 10 g, Na 2 HP0 4 x 12 H 2 0 1 g, KH 2 P0 4 1.5 g, MgS0 4 0.5 g, per 1 L, 1 g yeast extract (Raper 1984). Another method of long-term storage of spores is liophylization.
  • amoebae or spores are stored short-term at 4°C in medium MS2 solidified with 10 g of agar per L.
  • the present invention also provides pharmaceutical
  • these preparations comprise one of the aforementioned amoebae/slugs or spores (Fig. 3), formulated for an administration to the patient.
  • amoebae, slugs or spores are incorporated into bandages, dressings, or other wound coverings.
  • spores are incorporated into salves, ointments, or other topical applications.
  • amoebae, slugs or spores are delivered by pharmaceutically acceptable carrier, that refers to any of the standard pharmaceutical carriers including, but not limited to, saline solution, water, emulsions (e.g., such as an oil/water or water/oil
  • compositions also can include stabilizers and preservatives.
  • stabilizers and preservatives for example, of carriers, stabilizers, and adjuvants.
  • the compositions of the present invention may be inoculated for horticultural or agricultural use. Such formulations include dips, sprays, seed dressings, stem injections, sprays, and mists.
  • compositions of the present invention may be administered in a number of ways depending upon whether local or systemic treatment is desired and upon the area to be treated. Administration may be topical (including ophthalmic and to mucous membranes including vaginal and rectal delivery), pulmonary (e.g., by inhalation or insufflation of powders or aerosols, including by nebulizer; intratracheal, intranasal, epidermal and transdermal), oral or parenteral. Parenteral administration includes intravenous, intraarterial, subcutaneous, intraperitoneal or intramuscular injection or infusion; or intracranial, e.g., intrathecal or intraventricular, administration.
  • compositions and formulations for topical administration may include transdermal patches, ointments, lotions, creams, gels, drops, suppositories, sprays, liquids and powders.
  • Conventional pharmaceutical carriers, aqueous, powder or oily bases, thickeners and the like may be necessary or desirable.
  • compositions and formulations for oral administration include powders or granules, suspensions or solutions in water or non-aqueous media, capsules, sachets or tablets.
  • Thickeners flavoring agents, diluents, emulsifiers, dispersing aids or binders may be desirable.
  • compositions and formulations for parenteral, intrathecal or intraventricular administration may include sterile aqueous solutions that may also contain buffers, diluents and other suitable additives such as, but not limited to, penetration enhancers, carrier compounds and other pharmaceutically acceptable carriers or excipients.
  • compositions of the present invention include, but are not limited to, solutions, emulsions, and liposome-containing formulations. These compositions may be generated from a variety of components that include, but are not limited to, preformed liquids, self-emulsifying solids and self-emulsifying semisolids.
  • the pharmaceutical formulations of the present invention may be prepared according to conventional techniques well known in the pharmaceutical industry. Such techniques include the step of bringing into association the active ingredients with the pharmaceutical carrier(s) or excipient(s). In general the formulations are prepared by uniformly and intimately bringing into association the active ingredients with liquid carriers or finely divided solid carriers or both, and then, if necessary, shaping the product.
  • compositions of the present invention may additionally contain other adjunct components conventionally found in pharmaceutical compositions.
  • the compositions may contain additional, compatible, pharmaceutically-active materials such as, for example, antipruritics, astringents, local anesthetics or anti-inflammatory agents, or may contain additional materials useful in physically formulating various dosage forms of the compositions of the present invention, such as dyes, flavoring agents, preservatives, antioxidants, opacifiers, thickening agents and stabilizers.
  • additional materials useful in physically formulating various dosage forms of the compositions of the present invention such as dyes, flavoring agents, preservatives, antioxidants, opacifiers, thickening agents and stabilizers.
  • such materials when added, should not unduly interfere with the biological activities of the components of the compositions of the present invention.
  • the formulations can be sterilized and, if desired, mixed with auxiliary agents, e.g., lubricants, preservatives, stabilizers, wetting agents, emulsifiers, salts for influencing osmotic pressure, buffers, colorings, flavorings and/or aromatic substances and the like which do not deleteriously interact with the active agents of the formulation.
  • auxiliary agents e.g., lubricants, preservatives, stabilizers, wetting agents, emulsifiers, salts for influencing osmotic pressure, buffers, colorings, flavorings and/or aromatic substances and the like which do not deleteriously interact with the active agents of the formulation.
  • Dosing is dependent on severity and responsiveness of the disease state or condition to be treated, with the course of treatment lasting from several days to several months, or until a cure is effected or a diminution of the disease state is achieved.
  • treatment is administered in one or more courses, where each course comprises one or more doses per day for several days (e.g., 1, 2, 3, 4, 5, 6) or weeks (e.g., 1, 2, or 3 weeks, etc.).
  • courses of treatment are administered sequentially (e.g., without a break between courses), while in other embodiments, a break of 1 or more days, weeks, or months is provided between courses.
  • treatment is provided on an ongoing or maintenance basis (e.g., multiple courses provided with or without breaks for an indefinite time period).
  • Optimal dosing schedules can be calculated from
  • the administering physician can readily determine optimum dosages, dosing methodologies and repetition rates.
  • Embodiments of the present invention provide compositions and methods for the therapeutic, clinical, research, agricultural and industrial use of amoebae. Exemplary applications are discussed herein. Additional uses are known to one of ordinary skill in the art.
  • amoebae are used in the treatment of subjects (e.g., humans or non-human animals) infected with a microorganism (e.g., pathogenic bacteria).
  • a microorganism e.g., pathogenic bacteria
  • amoebae are used on infected skin wounds. At sites suffering tissue damage and infection, amoebae will consume large numbers of pathogens. This feeding behavior reduces the bacterial load sufficiently for wounds and surgical closures to heal naturally, and for grafts to thrive.
  • Biotherapeutics for disease can be found in bacteriophage, bacterial interference, and leech and maggot therapies.
  • bacteriophage therapy as an alternative or adjunct to chemical antibiotics, has been advanced in Eastern Europe. Presently, this strategy is receiving renewed attention in Great Britain and in the United States.
  • Phage therapy uses mixtures of lytic viruses to kill pathogenic bacteria (Mann NH, 2008. Res Microbiol. 159:400-405).
  • a second strategy, bacterial interference uses live benign bacteria to displace pathogenic organisms.
  • biologies are much broader than those examples mentioned above.
  • preparations of the prokaryote Lactobacillus acidophilus for use in human therapies is known (see, e.g., US Patent Nos. 5,032,399 and 5,733,568).
  • pharmaceutical preparations of Lactobacillus acidophilus are known (See e.g., US Patent No. US 4314995). Additional applications of biologies in human therapy are described in US Patent Nos.
  • amoebae are utilized in the treatment of microbial infections in mucus membranes (e.g., nostrils, throat, rectum, vagina, etc.), tissues or organs (e.g., urinary tract, etc) or bodily fluids (e.g., blood).
  • mucus membranes e.g., nostrils, throat, rectum, vagina, etc.
  • tissues or organs e.g., urinary tract, etc
  • bodily fluids e.g., blood
  • amoebae are utilized in the treatment of infection by drug or multi-drug resistant bacteria (e.g., methycillin resistant Staph Aureus (MRSA) or MDR (multi-drug resistant) Acinetobacter baumannii) or dormant persister cells.
  • drug or multi-drug resistant bacteria e.g., methycillin resistant Staph Aureus (MRSA) or MDR (multi-drug resistant) Acinetobacter baumannii
  • MRSA methycillin resistant Staph Aureus
  • MDR multi-drug resistant Acinetobacter baumannii
  • Dormant persister cells are tolerant to antibiotics and are largely responsible for recalcitrance of chronic infections. Chronic infections are often caused by pathogens that are susceptible to antibiotics, but the disease may be difficult or even impossible to eradicate with antimicrobial therapy. For many pathogens, including S. aureus, a highly significant factor of virulence steams from the fact that in addition to fast-growing cells these pathogens produces small numbers of dormant persister cells whose function is survival in adverse circumstances. Persisters are not mutants, but phenotypic variants of the wild type, and are tolerant to killing by antibiotics. The dormancy protection from antibiotics is mechanistically distinct from genetically determined MRSA.
  • SCVs Small Colony Variants
  • SCVs have been found for many genera of bacteria, but they have been most extensively studied for staphylococci. (Proctor et al, Clin. Infect. Dis. 20, 95-102 (1995). S. aureus SCVs can also cause more aggressive infections in both humans and animals.
  • the high rate of selection by aminoglycosides indicates that SCVs are part of the normal life cycle of staphylococci. (Massey et al., Curr. Biol. 11, 1810-1814 (2001). Massey, R. C. & Peacock, S. J. Curr. Biol. 12, R686-R687 (2002).
  • Experiments conducted during the course of development of embodiments of the present invention demonstrated that soil amoebae can destroy MRSA and persister cells of the pathogen.
  • the present methods and compositions are directed to specifically controlling (e.g., therapeutic treatments or prophylactic measures) diseases caused by the following pathogens: Bartonella henselae, Borrelia burgdorferi,
  • compositions of the present invention are used to treat surfaces.
  • Surfaces that can be treated by the methods and compositions of the present invention include but are not limited to, surfaces of a medical device (e.g., a catheter, implants, stents, etc.), a wound care device, a body cavity device, a human body, an animal body, a food preparation surface, an industrial surface, a personal protection device, a birth control device, and a drug delivery device.
  • a medical device e.g., a catheter, implants, stents, etc.
  • a wound care device e.g., a wound care device, a body cavity device, a human body, an animal body, a food preparation surface, an industrial surface, a personal protection device, a birth control device, and a drug delivery device.
  • Surfaces include but are not limited to silicon, plastic, glass, polymer, ceramic, skin, tissue, nitrocellulose, hydrogel, paper, polypropylene, cloth, cotton, wool, wood, brick, leather, vinyl, polystyrene, nylon, polyacrylamide, optical fiber, natural libers, nylon, metal, rubber, soil and composites thereof.
  • the treating destroys growing, nongrowing, or dormant microbial pathogens.
  • amoebae are used in the treatment of microbial infections of agricultural and industrial plants.
  • amoebae were shown to be effective against virulent strains of Erwinia amylovora (88, 85.1 and A97.1) a causative agent of Fire blight in fruit crops.
  • Burkholderia cepacia is a bacterium which produces economic losses to onion crops (Burkholder 1950. Phytopathology 40: 115-118).
  • the methods and compositions of the present invention target bacteria present as a biofilm.
  • Biofilms can be broadly defined as microbial cells attached to a surface, and which are embedded in a matrix of extracellular polymeric substances produced by the microorganisms. Biofilms are known to occur in many environments and frequently lead to a wide diversity of undesirable effects. For example, biofilms cause fouling of industrial equipment such as heat exchangers, pipelines, and ship hulls, resulting in reduced heat transfer, energy loss, increased fluid frictional resistance, and accelerated corrosion. Biofilm accumulation on teeth and gums, urinary and intestinal tracts, and implanted medical devices such as catheters and prostheses frequently lead to infections (Characklis WG.
  • Biofilm formation is a serious concern in the food processing industry because of the potential for contamination of food products, leading to decreased food product quality and safety (Kumar CG and Anand SK, Int J Food Microbiol 1998; 42:9-27; Wong, J Dairy Sci 1998; 81 :2765-70; Zottola and Sasahara, Int J Food Microbiol 1994; 23: 125-48).
  • the surfaces of equipment used for food handling or processing are recognized as major sources of microbial contamination. (Dunsmore et al., J Food Prot 1981; 44:220-40; Flint et al, Biofouling 1997; 11 :81-97; Grau, In: Smulders FJM ed.
  • Biofilm bacteria are generally hardier than their planktonic (free-living) counterparts, and exhibit increased resistance to antimicrobial agents such as antibiotics and disinfectants. It has been shown that even with routine cleaning and sanitizing procedures consistent with good manufacturing practices, bacteria can remain on equipment, food and non-food contact surfaces and can develop into bio films. In addition, L. monocytogenes attached to surfaces such as stainless steel and rubber, materials commonly used in food processing environments, can survive for prolonged periods (Helke and Wong, J Food Prot 1994; 57:963-8).
  • Phagocytic predation on bacteria by host immune cells shares a number of cellular mechanisms with free-living protozoa.
  • bacteria growing in biofilms appear to be less vulnerable to phagocytic predators than planktonic cells.
  • Widespread resistance against predators is mediated by the interplay of bio film- specific traits such as substratum adherence, exopolymer production, cellular cooperation, inhibitor secretion, and phenotypic variation.
  • inventions of the present invention provide compositions and methods for the use of amoebae in the killing of bacteria present in biofilms.
  • compositions for use in killing microorganisms utilize two or more distinct species of amoebae. Some species of amoebae use different chemoattractants while other species use the same attractants. For example, for D. mucoroides it is cyclic AMP, while that of P. violaceum is a dipeptide called glorin. This means that when the aggregation centers are first formed, each species is producing its own attractant and will attract only the amoebae that respond to it; they will have no interest in the attractant of the other species and therefore no possibility of commingling.
  • Raper and Thorn chose two species that had the same chemoattractant, which is cyclic AMP (Raper, K. B., and C. Thorn (1941) Am. J Botany 28: 69-78). Strains were D. mucoroides with white sori and D. purpureum with purple sori. The authors found that these two species co-aggregated into common centers, but there was a surprising sequel. Fruiting bodies arose from the same mound and their sorocarps were either white or purple: the amoebae had separated into two groups in the mound, and the resulting fruiting bodies were pure and all their amoebae were of either one species or the other.
  • H. Hagiwara Hagiwara, H. (1989) The taxonomic study of Japanese Dictyostelid cellular slime molds. Tokyo: National Science Museum Press
  • a strain of P. pallidum that produces a substance that destroys many other strains of P. pallidum as well as a common wild-type strain D. discoideum. They do so by secreting a lethal molecule that devastates the amoebae of the susceptible victim.
  • two or more compatible species are utilized in a composition. Such combinations are contemplated to find particular use in the killing of drug resistant microorganisms and mixed populations of microorganisms.
  • one or more amoebae are administered in combination with known anti-microbial agents.
  • antimicrobial agents There are an enormous amount of antimicrobial agents currently available for use in treating bacterial and fungal.
  • the skilled artisan is referred to Goodman & Gilman's "The Pharmacological Basis of Therapeutics" Eds.
  • these agents include agents that inhibit cell wall synthesis ⁇ e.g., penicillins, cephalosporins, cycloserine, vancomycin, bacitracin); and the imidazole antifungal agents ⁇ e.g., miconazole, ketoconazole and clotrimazole); agents that act directly to disrupt the cell membrane of the microorganism ⁇ e.g., detergents such as polmyxin and colistimethate and the antifungals nystatin and amphotericin B); agents that affect the ribosomal subunits to inhibit protein synthesis ⁇ e.g., chloramphenicol, the tetracyclines, erthromycin and clindamycin); agents that alter protein synthesis and lead to cell death ⁇ e.g., aminoglycosides); agents that affect nucleic
  • amoebic therapy is unorthodox.
  • Various publications report the typical growth conditions for amoebae isolates: solid media composed of natural product extracts, soil bacteria (food source), and 22°C incubation at atmospheric oxygen (Raper KB, Rahn AW. (1984) The Dictyostelids).
  • wounded tissue is at an elevated temperature (Ring EFJ. 1986). Bioeng Skin 2(1): 15-30; Forage AV. (1964) Br J Plast Surg 17: 60-1; McGuiness W, Vella E, Harrison D. (2004) J Wound Care 13(9): 383-5) or hypoxic (Mathieu D.
  • the bacterial species employed in the work were all clinical/field isolates of common pathogens (e.g., Klebsiella pneumoniae, Staphylocococcus aureus (including its MRSA derivative), Erwinia amylowora, Pseudomonas syringie).
  • the screens identified a group of amoebae that consume all tested pathogens under the proxy conditions, thus making them suitable for biotherapeutic uses.
  • Preferred candidates are those which most vigorously devour the test bacteria - in other words, the amoebae producing the largest clearing zones on lawn of specific bacteria.
  • the amoebae should have the ability to: consume the test bacteria, whether growing or not growing, grow/divide at the elevated temperature, grow/divide under hypoxic conditions, and grow/divide in the presence of sera.
  • Petri-dish assay for the efficiency of amoebic feeding and development: To identify putative therapeutic amoebae, a Petri-dish growth assay was used. This assay resembles a bacteriophage growth and enumeration assay in which mixtures of phage and susceptible bacteria are co-cultured as monolayers on solid medium. Each bacteriophage-infected cell gives rise to a clear plaque within the lawn of bacteria. As seen in Figures 1 and 4, similar zones of clearing are observed when WS646 amoebae are co-cultured with bacteria.
  • mixtures of amoebae (or spores) and test pathogens are co-cultured on solid medium (bacterial lawns) or resuspended in semi-solid agar. If the amoebae digest the pathogens, plaques or clearing zones appear on the lawn as the amoebae consume the bacteria. The size of the clear zones is recorded as a measure of the rate of amoebic feeding (compare Fig. 1 and Fig. 4).
  • Bacterial pathogens were grown in SM2 broth (e.g., E. amylovora) or other growth supporting medium (e.g. Tryptic Soy Broth, S. aureus) and organisms were removed from the medium by centrifugation. The bacterial cell pellets from these cultures were then plated on the surface of solid medium or resuspended in pre-warmed semi-solid medium (containing 0.6-1% agar). Then spores or amoebae themselves were spotted on lawns of test bacteria and after incubation (e.g., at a desired temperature, presence/absence of serum) photographed without or with magnification, and with or without a light diffuser, using various types of photographic equipment (indicated in the Fig.
  • SM2 broth e.g., E. amylovora
  • other growth supporting medium e.g. Tryptic Soy Broth, S. aureus
  • microaerophylic conditions were created using microbiological tubes containing growth supporting microbiological media.
  • pathogens e.g. E. amylovora
  • pathogens were grown in SM2 semi solid medium, which was impregnated with a pear slice or supplemented with a homogenized pear according to the established protocols (Vanneste,et al. 1990 J. Bact., 1990, p. 932-941 Vol. 172; Won-Sik Kim et al, Microbiology (2004), 150, 2707-2714).
  • This example describes the used of two or more types of amoebae to assure that the treated surface/tissue becomes microorganism-free (other than the presence of amoebae themselves, or their various social stages of development; e.g. slugs or sorocarps).
  • amoebae isolates e.g., Salvador, and WS647 or WI321.7 and WS142
  • their combination is suitable for use in a biotherapeutic cocktail of amoebae.
  • amoebae isolates show a very strong antagonistic behavior (e.g. WS255 x281 and WS647 or WS321.5 and either FR14 or WS142) as evidenced by the non-overlapping clearing zones they produce.
  • Example 3
  • amoebae are propagated at a temperature between 21 - 25 °C (Raper KB. (1951) Q Rev Biol 26(2): 169-90; Raper KB, Rahn AW. (1984) The Dictyostelids).
  • Temperatures above 25 °C can inhibit the growth of many species of amoebae. Such species can be employed in many, perhaps all agricultural applications (e.g., against E. amylovora or P. syringiae). Although dermatological wounds typically have comparable surface temperatures (between 24 - 26°C), they can measure 35°C or higher (Ring EFJ. (1986) Bioeng Skin 2(1): 15-30; Forage AV. (1964) Br J Plast Surg 17: 60-l;McGuiness W, Vella E, Harrison D. (2004) J Wound Care 13(9): 383-5). In published reports, the determination of growth temperatures relied on observing fruiting body formation, not the ability of free-living amoeba to feed on bacteria.
  • amoebae were identified that can grow at temperatures of 30°C (WS371A, WS321.5, Ws321.7, WS309, WS142, WS255x281) or even 37°C (Salvador) whereas most of the amoebae tested grew only at room temperature (Tu4b, X3, Turkey 27 WS57.7, FR4, WS647).
  • Such temperature-resistant strains e.g. Salvador
  • amoebae will encounter hypoxic conditions because of inflammation, edema and compromised vasculature (Mathieu D. (2006) Int J Low Extrem Wounds 5(4): 233-5). Amoebae are known to grow well in the presence of oxygen and have been reported to become quiescent under anaerobic conditions (Bonner JT. (2009) The social amoebae: the biology of cellular slime molds, ix, 144 p.). However, except for a single study on the development of submerged isolates of D. mucoroides, the tolerance of amoebae to anoxic environments appears not to have been formally investigated (Sternfeld et al, (1977) Proc Natl Acad Sci U S A 74(1): 268-71).
  • Figures 10- 13 demonstrate that selected amoebae isolates can feed on several species of bacterial pathogens in the absence or presence of bovine or porcine sera. Furthermore, they can feed on bacteria re-suspended in media supporting or not supporting their growth.
  • Figure 10 shows feeding of amoebae on MRS A.
  • the plates were made by using the pathogen grown overnight in TSB medium. Bacteria were peleted and resuspended in semi- solid agar containing bovine serum diluted seven-fold in semi-solid agar supplemented with 0.9% sodium chloride. Plates were incubated at 35°C and data was recorded after 48 hours. Plates were photographed using a camera attached to a Olympus microscope at 8X
  • Clearing zones indicate lawns of bacteria destroyed by feeding and dividing amoebae. Structures inside are showing aggregation, slugs and mature fruiting bodies of amoebae with spores. Photos were taken without a light diffuser in the microscope resulting in an enhanced contrast between clearing zones and confluent bacterial growth.
  • Figure 11 shows a comparison of the feeding of amoebae on Klebsiella pneumoniae with and without serum.
  • Column A shows zones of growth (or lack thereof) of amoebae on plates inoculated with Klebsiella pneumoniae. The plates were made by using the pathogen grown overnight in SM2 medium. Bacteria were peleted and resuspended in semi-solid agar containing 0.9% sodium chloride and seven-fold diluted bovine serum (column A) or in semisolid medium without bovine serum (Column B). Plates were incubated at room temperature and data was recorded after 48 hours (Clearing). Plates were photographed using a camera attached to an Olympus microscope at 8X magnification. Clearing zone shows feeding front of amoebae and structures inside are showing aggregation, slugs and mature fruiting bodies of amoebae with spores.
  • Figure 12 shows feeding of amoebae on a menD mutant of S. aureus in the presence and absence of serum. Shown are pictures of amoebae feeding on the menD mutant.
  • the plates were made by using the pathogen grown overnight in TSB medium. Bacteria were peleted and resuspended in semi-solid agar containing 0.9% sodium chloride without bovine serum (Column A) and seven-fold diluted bovine serum (column B). Each set of the plates was supplemented with either soft agar (left) or SM2 medium (right). Plates were incubated at room temperature and data was recorded after 48 hours (Clearing). Plates were
  • Clearing zone shows feeding front of amoebae and structures inside are showing aggregation, slugs and mature fruiting bodies of amoebae with spores.
  • Photos in a column marked as (“non nutrient agar") were taken without a light diffuser in the microscope. Therefore, contrast between clearing zones and confluent bacterial growth is enhanced in comparison to the two panels in the column A (absence of serum).
  • Figure 13 shows feeding of amoebae on Wide Type Staphylococcus in the presence or absence of serum. Shown are pictures of amoebae feeding on the mend+ strain of S. aureus. The plates were made by using the pathogen grown overnight in TSB medium. Bacteria were peleted and resuspended in semi-solid agar containing 0.9% sodium chloride without bovine serum (Column A) and seven-fold diluted bovine serum (column B). Each set of the plates was supplemented with either soft agar (left) or SM2 medium (right). Plates were incubated at room temperature and data was recorded after 48 hours (Clearing). Plates were
  • Clearing zone shows feeding front of amoebae and structures inside are showing aggregation, slugs and mature fruiting bodies of amoebae with spores.
  • Photos in a column marked as (“non nutrient agar") were taken without a light diffuser in the microscope. Therefore, contrast between clearing zones and confluent bacterial growth is enhanced in comparison to the two panels in the column A (absence of serum).
  • Feeding was not affected or minimally effected by serum with the following amoebae: WS321.7, WS255x281, Frl4. Modest inhibition by serum was observed with the following amoebae Turkey 27, WS57.7, WS371A, X3 WS309. Poor or no growth was observed with the Salvador strain of amebae.
  • FIG. 8 shows feeding of amoebae on natural isolates of virulent strains of Erwinia amylovora (88, 85.1 and A97.1) a causative agent of Fire blight in fruit crops.
  • Column A presents feeding and development of amoebae in the presence of Erwinia amylovora virulent isolates.
  • Figure 15 shows feeding of amoebae on natural isolate virulent agent of bean disease
  • Pseudomonas syringe 207.2 Pseudomonas syringe 207.2.
  • Column A shows zones of growth (or lack thereof) of amoebae on plates inoculated with P. syringiae 207.2.
  • the plates were prepared by using the pathogen grown overnight in SM2 medium. Bacteria were peleted and resuspended in semi-solid agar containing MS2 nutrient agar (column A) or non nutrient agar (Column B). Plates were incubated at room temperature and data was recorded after 48 hours (Clearing). Plates were photographed using a camera attached to an Olympus microscope at 8X magnification.

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Abstract

La présente invention concerne des amibes (moules de biofilm) et leurs utilisations. En particulier, la présente invention concerne l'utilisation d'amibes ou de leurs spores stables dans l'environnement en vue de traiter des infections microbiennes, l'invention concernant également d'autres d'utilisations.
PCT/US2011/039110 2010-06-03 2011-06-03 Amibes thérapeutiques et leurs utilisations WO2011153460A2 (fr)

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WO2021133800A1 (fr) * 2019-12-23 2021-07-01 Amebagone, Llc Composition thérapeutique et ses utilisations

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EP2575833B1 (fr) 2018-03-21
US20110300106A1 (en) 2011-12-08
US8715641B2 (en) 2014-05-06
EP2575833A2 (fr) 2013-04-10
US20140030227A1 (en) 2014-01-30
WO2011153460A3 (fr) 2012-04-19
EP2575833A4 (fr) 2013-11-13
US8551471B2 (en) 2013-10-08

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